Brain Metastasis of Pheochromocytoma: Diagnostic and Therapeutic Challenge.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 31260853.
- Also identified by DOI 10.1016/j.wneu.2019.06.163.
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Abstract
Pheochromocytoma brain metastasis is extremely rare. Few cases have been reported in the literature. Therefore, diagnosis and effective treatment of these lesions are difficult. Here, we report the case of 29-year-old woman, who was operated on for a right adrenal pheochromocytoma. Fourteen months later, a posterior fossa tumor was diagnosed. Radiologic findings mimicked an extra-axial lesion. The radiologic differential diagnosis was difficult even using magnetic resonance imaging spectroscopy. The patient was operated on through a retrosigmoid approach. Local recurrence occurred 6 months after first surgery. The patient died 1 month later, despite a second operation. Although the occurrence of brain metastases in pheochromocytoma is not prevalent, patients presenting with suggestive features need to be carefully considered. Magnetic resonance imaging can help in differential diagnosis with a primary brain tumor. There are no established guidelines for the treatment of pheochromocytoma brain metastasis, for which the prognosis remains dismal, despite effective surgery.
Medical subject headings
- Adrenal Gland Neoplasms
- Infratentorial Neoplasms
- Pheochromocytoma